Canonical Allele Identifier: PA2827383785
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 373239
ClinVar RCV Id: RCV000413165 RCV003505108
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333649.1:p.Pro346Leu
CA4348533
NM_001346720.2:c.1037C>T